University of Arkansas System este un sistem universitar public la nivel de stat, care sprijină accesul la educație, cercetarea, serviciile de sănătate și implicarea în comunitate în întregul stat Arkansas. Înființat în 1871, acesta reunește universități, colegii comunitare și instituții specializate care contribuie la dezvoltarea economică, educațională și culturală a statului. Activitatea sistemului acoperă predarea, cercetarea, administrația și implicarea publică și este ghidată, printre altele, de planul său strategic Transformation 2025. Rețeaua sa extinsă oferă oportunități persoanelor interesate să contribuie la învățământul superior și la numeroasele servicii furnizate de instituțiile sale.
Clinical Research Nurse I–III, Cancer Trials
Coordinate cancer clinical trials at UAMS, an academic health and research center. Support participants, regulatory compliance, research data, and study teams.
Descriere
- Coordinate participant screening, consent, enrollment, treatment, observation, and follow-up for cancer trials.
- Keep physicians and participants on schedule through each treatment phase and aligned with study requirements.
- Advise the principal investigator on study procedures and data collection needs.
- Represent the department and investigators at local, regional, and national meetings.
- Coordinate communication among staff, investigators, research and clinical professionals, UAMS leaders, and study sponsors.
- Create, implement, and maintain quality assurance plans and standard operating procedures.
- Act as an administrator and liaison for the principal investigator, participants, compliance teams, research and clinical professionals, and funding organizations.
- Maintain compliance with regulations, including serious adverse event reporting.
- Prepare written materials, analyze data, and develop conclusions.
- Maintain clinical and research records and database entries for participants on assigned protocols.
- Assess patients for study eligibility before enrollment.
- Review clinical care and confirm study procedures meet protocol requirements.
- Educate patients and their families or caregivers, and support physicians with patient management.
- Help participants follow study protocols.
- Collect and manage patient information with the CRN Team Lead and clinical research associates.
- Check clinical research associate data entries for accuracy and completeness; help resolve queries and support monitoring and audit visits.
- Train staff and investigators.
- Develop and introduce process improvements and electronic infrastructure.
- Complete ongoing professional training.
- Perform other assigned duties.
Cerințe
- Registered nurse.
- Level I: Three years of general nursing and/or general research experience.
- Level II: Three years of general research experience, with demonstrated skill in study planning and development, research nursing, and research patient management.
- Level III: At least five years of clinical research experience, with demonstrated skill in study planning and development, research nursing, and research patient management.
- Level III: CCRP, CCRC, or equivalent professional certification required at hire.
- Obtain CRS certification within two years of hire.
- Proof of legal authorization to work in the United States is required on the first day of employment.
- License or certificate required to apply.
- Pre-employment screening may include criminal background, drug, and education checks.
- Preferred: Bachelor of Science in Nursing.
- Preferred: Oncology experience.
- Preferred: Clinical research experience.
Beneficii
- Medical, dental, and vision plans are available for eligible staff and family members.
- Holiday, vacation, and sick leave.
- Undergraduate tuition discounts for staff and dependents.
- UAMS matching contributions of up to 10%.
- Basic life insurance coverage up to $50,000.
- Career training and educational opportunities.
- Merchant discounts.
- Concierge prescription delivery on the main campus for prescriptions filled through the UAMS pharmacy.